FDA Inspection 719827 — InfoRLife SA

InfoRLife SA — FEI 3004537783

The FDA completed an inspection of InfoRLife SA on April 5, 2011 in Campascio. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 5, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Campascio (Switzerland)